Milner, P F <br/><br/>
Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain.  [electronic resource] 

 -  Lancet (London, England)  Apr 1971 
 - 729-32 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0140-6736 
<br/><br/><label>Standard No.: </label>10.1016/s0140-6736(71)91992-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Electrophoresis<br/>Female<br/>Hemoglobinopathies--genetics<br/>Hemoglobins, Abnormal--analysis<br/>Heterozygote<br/>Humans<br/>Male<br/>Methods<br/>Middle Aged<br/>Pedigree<br/>Thalassemia--genetics